Preferred Label : chromosomes;
UMLS semantic type : T026 - Cell Component;
Origin ID : M0004414;
UMLS CUI : C0008633;
Automatic exact mappings (from CISMeF team)
- Currated CISMeF NLP mapping
- Related record
- Semantic type(s)
http://www.eaclf.org/docs/TestADNlc-Notice_final.pdf
2024
France
patient education handout
Last Screening
information dissemination
pregnancy, nos
Destination
Circulating Cell-Free DNA
emigration and immigration
Informative
mass screening
Screening Study
Cytogenetic Abnormality
Substance Screening
Chromosome Disorder
Cell-Free DNA Blood Collection Tube
dna analysis, nos
DNA Analysis
chromosomal disease, nos
cfDNA Mutation
Informed
Pregnant People
DNA
Gravida
Genetic Screening
Cell-Free Nucleic Acids
Human Cells, Tissues, and Cellular and Tissue-Based Products Screening
chromosome analysis, nos
Cancer Screening
Trial Screening
Eligibility Determination
Site Screening
No Information Available
screening
chromosomes
chromosome aberrations
Oprelvekin
---
https://www.has-sante.fr/jcms/p_3545370/fr/examens-bases-sur-l-adn-libre-circulant-realises-dans-le-cadre-du-depistage-de-la-trisomie-21-opportunite-du-reperage-d-autres-anomalies-chromosomiques
2024
France
public health guidelines
chromosome aberrations
Cell-Free Nucleic Acids
trisomy
mass screening
deoxyribonucleic acid, nos
DNA
down syndrome
chromosomal disease, nos
achievement
screening
chromosomes
---
https://www.has-sante.fr/jcms/p_3373681/fr/syndrome-de-duplication/deletion-inversee-du-bras-court-du-chromosome-8
2022
France
practice guideline
chronic disease, nos
chronic disease
Diseases
Handbook
arm
chromosomes, human, pair 8
Chronic disease
chromosomes
inversion
---
http://www.eaclf.org/docs/GBP-ADNlc-V3.pdf
2017
false
false
false
France
French
practice guideline
screening
deoxyribonucleic acid, nos
fetus, nos
recommendations, health planning
chromosomal disease, nos
chromosomes
circulating
version, nos
DNA
fetus
directive counseling
data collection
diagnosis
chromosome aberrations
---
